Cytosolic pH Regulates Cell Growth through Distinct GTPases, Arf1 and Gtr1, to Promote Ras/PKA and TORC1 Activity

被引:95
作者
Dechant, Reinhard [1 ,2 ]
Saad, Shady [1 ,3 ]
Ibanez, Alfredo J. [4 ]
Peter, Matthias [1 ,2 ]
机构
[1] ETH, Inst Biochem, CH-8093 Zurich, Switzerland
[2] Competence Ctr Syst Physiol & Metab Dis, CH-8093 Zurich, Switzerland
[3] Life Sci Zurich, PhD Program Syst Biol Complex Dis, CH-8093 Zurich, Switzerland
[4] ETH, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
VACUOLAR H+-ATPASE; TRANSFER-RNA SYNTHETASE; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTORS; NUCLEAR-LOCALIZATION; RAG GTPASES; AMINO-ACIDS; EGO COMPLEX; YEAST; PROTEIN;
D O I
10.1016/j.molcel.2014.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of cell growth by nutrients is governed by highly conserved signaling pathways, yet mechanisms of nutrient sensing are still poorly understood. In yeast, glucose activates both the Ras/PKA pathway and TORC1, which coordinately regulate growth through enhancing translation and ribosome biogenesis and suppressing autophagy. Here, we show that cytosolic pH acts as a cellular signal to activate Ras and TORC1 in response to glucose availability. We demonstrate that cytosolic pH is sensitive to the quality and quantity of the available carbon source (C-source). Interestingly, Ras/PKA and TORC1 are both activated through the vacuolar ATPase (V-ATPase), which was previously identified as a sensor for cytosolic pH in vivo. V-ATPase interacts with two distinct GTPases, Arf1 and Gtr1, which are required for Ras and TORC1 activation, respectively. Together, these data provide a molecular mechanism for how cytosolic pH links C-source availability to the activity of signaling networks promoting cell growth.
引用
收藏
页码:409 / 421
页数:13
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